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FDA 510(k)

HEX tanning booth

K-Number: K152336 · 2016-05-02

ApplicantJ & B Products Ltd Dba Hex Tanning
Decision Date2016-05-02
Product CodeLEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HEX tanning booth is the device name listed in this FDA 510(k) record. The listed applicant is J & B Products Ltd Dba Hex Tanning. It received FDA 510(k) clearance on 2016-05-02 under 510(k) number K152336. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEX tanning booth?

HEX tanning booth is a medical device that received FDA 510(k) clearance on 2016-05-02. The listed applicant is J & B Products Ltd Dba Hex Tanning. The 510(k) number is K152336.

When did HEX tanning booth receive FDA 510(k) clearance?

HEX tanning booth received FDA 510(k) clearance on 2016-05-02, under 510(k) number K152336.

Who is the listed applicant for HEX tanning booth?

The FDA 510(k) record lists J & B Products Ltd Dba Hex Tanning as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEX tanning booth?

The FDA product code for HEX tanning booth is LEJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: LEJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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